3-Bromo-2-methyl-1H-quinolin-4-one

Base Information

Chemical Name:3-Bromo-2-methyl-1H-quinolin-4-one
CAS No.:41999-24-0
Molecular Formula:C₁₀H₈BrNO
Molecular Weight:238.084
Hs Code.:
Mol file:41999-24-0.mol

Synonyms:3-bromo-2-methylquinolin-4(1H)-one

Suppliers and Price of 3-Bromo-2-methyl-1H-quinolin-4-one

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Crysdot
3-Bromo-2-methylquinolin-4(1H)-one 97%
1g
$ 376.00

Crysdot
3-Bromo-2-methylquinolin-4(1H)-one 97%
5g
$ 972.00

Crysdot
3-Bromo-2-methylquinolin-4(1H)-one 97%
10g
$ 1439.00

Chemenu
3-Bromo-2-methylquinolin-4(1H)-one 97%
10g
$ 1356.00

Chemenu
3-Bromo-2-methylquinolin-4(1H)-one 97%
5g
$ 916.00

Chemenu
3-Bromo-2-methylquinolin-4(1H)-one 97%
1g
$ 355.00

Total 3 raw suppliers

Chemical Property of 3-Bromo-2-methyl-1H-quinolin-4-one

Chemical Property:

Purity/Quality:

99% ^*data from raw suppliers

3-Bromo-2-methylquinolin-4(1H)-one 97% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Uses 3-Bromo-2-methyl-4-quinolone is Quinolone and Quinoline derivative and analog having antiparasitic or anti-infectious activity.

Technology Process of 3-Bromo-2-methyl-1H-quinolin-4-one

There total 4 articles about 3-Bromo-2-methyl-1H-quinolin-4-one which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 96.0%

: 5660-24-2
2-methyl-1H-quinolin-4-one

: 41999-24-0
3-bromo-2-methylquinolin-4(1H)-one

Guidance literature:: With bromine; potassium bromide; sodium hydroxide; In water; at 20 ℃;
DOI:10.1021/jm1007903

Reference yield:

: 62-53-3
aniline

: 41999-24-0
3-bromo-2-methylquinolin-4(1H)-one

Guidance literature:: Multi-step reaction with 2 steps

1.1: acetic acid / benzene / 18 h / 100 °C / Inert atmosphere

1.2: Reflux; Inert atmosphere

2.1: bromine; potassium bromide; sodium hydroxide / water / 20 °C / Inert atmosphere

With bromine; acetic acid; potassium bromide; sodium hydroxide; In water; benzene; 1.1: Conrad-Limpach synthesis / 1.2: Conrad-Limpach synthesis;
DOI:10.1021/jo1014504

Reference yield:

: 6287-35-0
ethyl 3-anilinocrotonate

: 41999-24-0
3-bromo-2-methylquinolin-4(1H)-one

Guidance literature:: Multi-step reaction with 2 steps

1: diphenylether / 2 h / 250 °C

2: acetic acid; N-Bromosuccinimide / dichloromethane / 4 h / 20 °C

With N-Bromosuccinimide; acetic acid; In diphenylether; dichloromethane;